Incidental findings - OMIM - NCBI

Incidental findings - OMIM - NCBI



From NIH OMIM

OMIM is a comprehensive, authoritative compendium of human genes and genetic phenotypes that is freely available and updated daily.

---

• Search OMIM for "Incidental findings" 

+173470 - INTEGRIN, BETA-3; ITGB3

THROMBOCYTOPENIA, NEONATAL ALLOIMMUNE, INCLUDED; NAIT, INCLUDED

Cytogenetic locations: 17q21.32

OMIM:

 

173470

Gene summaries Genetic tests Medical literature

Select item 6026682.

#602668 - MYOTONIC DYSTROPHY 2; DM2

Cytogenetic locations: 3q21.3

OMIM:

 

602668

Gene summaries Genetic tests Medical literature

Select item 1622003.

#162200 - NEUROFIBROMATOSIS, TYPE I; NF1

Cytogenetic locations: 17q11.2

OMIM:

 

162200

Gene summaries Genetic tests Medical literature

Select item 2136004.

#213600 - BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 1; IBGC1

Cytogenetic locations: 8p11.21

OMIM:

 

213600

Gene summaries Genetic tests Medical literature

Select item 1900705.

*190070 - V-KI-RAS2 KIRSTEN RAT SARCOMA VIRAL ONCOGENE HOMOLOG; KRAS

V-KI-RAS1 PSEUDOGENE, INCLUDED; KRAS1P, INCLUDED

Cytogenetic locations: 12p12.1

OMIM:

 

190070

Gene summaries Genetic tests Medical literature

Select item 1917406.

*191740 - UDP-GLYCOSYLTRANSFERASE 1 FAMILY, POLYPEPTIDE A1; UGT1A1

UDP-GLYCOSYLTRANSFERASE 1 FAMILY, POLYPEPTIDE A GENE COMPLEX, INCLUDED; UGT1A@, INCLUDED

Cytogenetic locations: 2q37.1

OMIM:

 

191740

Gene summaries Genetic tests Medical literature

Select item 1123507.

%112350 - WEISMANN-NETTER SYNDROME; WNS

OMIM:

 

112350

Gene summaries Genetic tests Medical literature

Select item 1140008.

#114000 - CAFFEY DISEASE

Cytogenetic locations: 17q21.33

OMIM:

 

114000

Gene summaries Genetic tests Medical literature

Select item 1094009.

#109400 - BASAL CELL NEVUS SYNDROME; BCNS

Cytogenetic locations: 9q22.32, 1pter-p36.13, 1p34.1

OMIM:

 

109400

Gene summaries Genetic tests Medical literature

Select item 26510010.

#265100 - PULMONARY ALVEOLAR MICROLITHIASIS

Cytogenetic locations: 4p15.2

OMIM:

 

265100

Gene summaries Genetic tests Medical literature

Select item 61716611.

#617166 - EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 47; EIEE47

Cytogenetic locations: 3q28-q29

OMIM:

 

617166

Gene summaries Genetic tests Medical literature

Select item 18780012.

#187800 - BLEEDING DISORDER, PLATELET-TYPE, 16; BDPLT16

Cytogenetic locations: 1pter-p36.13, 17q21.31

OMIM:

 

187800

Gene summaries Genetic tests Medical literature

Select item 60421313.

#604213 - CHUDLEY-MCCULLOUGH SYNDROME; CMCS

Cytogenetic locations: 1p13.3

OMIM:

 

604213

Gene summaries Genetic tests Medical literature

Select item 60527014.

*605270 - N-SULFOGLUCOSAMINE SULFOHYDROLASE; SGSH

Cytogenetic locations: 17q25.3

OMIM:

 

605270

Gene summaries Genetic tests Medical literature

Select item 15080015.

#150800 - HEREDITARY LEIOMYOMATOSIS AND RENAL CELL CANCER; HLRCC

Cytogenetic locations: 1q43

OMIM:

 

150800

Gene summaries Genetic tests Medical literature

Select item 10580016.

%105800 - ANEURYSM, INTRACRANIAL BERRY, 1; ANIB1

Cytogenetic locations: 7q11.2

OMIM:

 

105800

Gene summaries Genetic tests Medical literature

Select item 60121517.

*601215 - ATR GENE; ATR

Cytogenetic locations: 3q23

OMIM:

 

601215

Gene summaries Genetic tests Medical literature

Select item 13005018.

#130050 - EHLERS-DANLOS SYNDROME, VASCULAR TYPE; EDSVASC

Cytogenetic locations: 2q32.2

OMIM:

 

130050

Gene summaries Genetic tests Medical literature

Select item 16780019.

#167800 - PANCREATITIS, HEREDITARY; PCTT

PANCREATITIS, CHRONIC, SUSCEPTIBILITY TO, INCLUDED

Cytogenetic locations: 7q31.2, 1pter-p36.13, 5q32, 1pter-p36.13, 1p36.21

OMIM:

 

167800

Gene summaries Genetic tests Medical literature

Select item 14651020.

#146510 - PALLISTER-HALL SYNDROME; PHS

Cytogenetic locations: 7p14.1

OMIM:

 

146510

Gene summaries Genetic tests Medical literature